Method for promoting efficiency of gene introduction into plant cells

ABSTRACT

A method for gene introduction by which higher efficiency for gene introduction than that by the conventional  Agrobacterium  method may be attained simply and without injuring the tissue is disclosed. According to the method of the present invention, the efficiency of gene introduction into plant cells by a bacterium belonging to genus  Agrobacterium  is promoted by accompanying centrifugation of the plant cells or plant tissue.

This application is a Divisional of co-pending application Ser. No. 12/902,631 filed on Oct. 12, 2010, which is a Continuation of application Ser. No. 10/089,696 filed on Apr. 3, 2002, which is a national phase of PCT Application No. PCT/JP00/05213 filed on Aug. 3, 2000, and for which priority of all the aforementioned applications is claimed under 35 U.S.C. §120; and this application claims priority of Application No. 158025/99 filed in Japan on Jun. 4, 1999, under 35 U.S.C. §119; the entire contents of all are hereby incorporated by reference.

TECHNICAL FIELD

The present invention relates to a method for promoting efficiency of gene introduction into plant cells.

BACKGROUND ART

The method for transformation using Agrobacterium has a number of excellent features including, in general, the high efficiency, the small number of copies of the introduced gene, the feature that the gene may be introduced without fragmenting a specific region called T-DNA, and the feature that the frequency of mutation occurred during cultivation is low because transformants may be obtained by cultivation for a short period of time. Therefore, the method is widely used as the most useful method for transforming various plants.

Although the Agrobacterium method is an extremely excellent method for transforming plants, whether the transformation is successful or not and the transformation efficiency largely varies depending on the plant species, genotype and the plant tissue used (Potrykus et al. 1998 (Reference (33))). That is, there are species with which the transformation has not been successful, and species with which the transformation may be attained only with limited varieties. Further, there are species with which the tissue to be used is limited so that a large amount of materials cannot be treated. To prepare a practical variety by genetic recombination, it is necessary to prepare a large number of transformed plants and to select the line having the desired character therefrom. However, at present, the type of plants with which a large number of transformed plants may be prepared for this purpose is limited. Thus, to develop an improved method by which this problem may be overcome is strongly demanded.

Although the method for transformation via Agrobacterium differs in the starting material, composition of the culture medium and the like, it is almost common to the Agrobacterium method that the method comprises making a tissue which is a starting material contact a suspension of Agrobacterium, selecting transformed cells after co-culturing, and growing transformed plants. The Agrobacterium is infected without performing a special treatment except for sterilization treatment which is carried out as required (Rogers et al. 1988 (Reference (34)), Visser 1991 (Reference (38)), McCormick 1991 (Reference (29)), Lindsey et al. 1991 (Reference (28))). Thus, studies for improving transformation system has been carried out mainly on the Agrobacterium strain, constitution of the vector, composition of medium, types of selection marker gene and promoter, the type of the tissue used as the material, and the like.

On the other hand, studies for changing the plant tissue before infection of Agrobacterium to a physiological state in which the genes are likely to be introduced have been scarcely made. If the physiological state of the tissue can be changed to such a physiological state by a simple treatment, the method is very useful, and it is expected that, in addition to the promotion of the transformation efficiency, transformation may be attained for the species or genotypes with which transformation has been hitherto difficult, that is a prominent effect. Known studies about pretreatment of plant tissue include particle gun treatment (Bidney et al., 1992 (Reference (5))) and ultrasonication treatment (Trick et al., 1997 (Reference (37))). Both of these methods aim at promoting invasion of bacteria into the plant tissue by physically injuring the tissue, so as to increase the number of plant cells infected. However, these methods are nothing more than developments of the leaf disk method (Horsch et al., 1985 (Reference (17))) and not treatments based on novel concepts. The degree of effectiveness and universality of the methods have not been clarified, and they are not used as general methods.

DISCLOSURE OF THE INVENTION

Accordingly, an object of the present invention is to provide a method for promoting efficiency of gene introduction into plant cells, by which gene introduction can be attained simply with a higher efficiency than the conventional gene introduction by Agrobacterium method, without injuring the tissue.

The present inventors intensively studied to discover that in the gene introduction method using Agrobacterium, the gene introduction efficiency may be significantly promoted by centrifuging the plant cells or plant tissue subjected to the gene introduction, thereby completing the present invention.

That is, the present invention provides a method for promoting efficiency of gene introduction into plant cells by a bacterium belonging to genus Agrobacterium, comprising centrifuging said plant cells or plant tissue.

By the present invention, a method for promoting efficiency of gene introduction into plant cells, by which gene introduction can be attained simply with a higher efficiency than the conventional gene introduction by Agrobacterium method, without injuring the tissue, has been provided. The method of the present invention may be applied to both monocotyledons and dicotyledons.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a drawing for showing a method for constructing pTOK233 which is an example of super-binary vectors, that may preferably be employed in the present invention.

FIG. 2 is a gene map of pSB133 which is an example of super-binary vectors, that may preferably be employed in the present invention.

FIG. 3 is a schematic view for showing the intermediate vector system and binary vector system which are major two vector systems of bacteria belonging to genus Agrobacterium.

FIG. 4 is a schematic view showing two binary vector systems derived from super virulent strain A281 of Agrobacterium tumefaciens.

In the above drawings, the following reference symbols denote the following meanings.

virB: the virB gene in the virulence region of Ti plasmid pTiBo542 contained in Agrobacterium tumefaciens A281

virC: the virC gene in the virulence region of Ti plasmid pTiBo542 contained in Agrobacterium tumefaciens A281

virG: the virG gene in the virulence region of Ti plasmid pTiBo542 contained in Agrobacterium tumefaciens A281

BL: left border sequence of T-DNA of bacteria belonging to genus Agrobacterium

BR: right border sequence of T-DNA of bacteria belonging to genus Agrobacterium

TC: tetracycline resistant gene

SP: spectinomycin resistant gene

IG: intron GUS gene

HPT: hygromycin resistant gene

K: restriction enzyme KpnI site

H: restriction enzyme HindIII site

Ampr: ampicillin resistant gene

BAR: bar gene

Pnos: promoter of nopaline synthetase gene

Tnos: terminator of nopaline synthetase gene

P35S: CaMV 35S promoter

COS, cos: COS site of λ phage

ORI, ori: replication origin of ColE1

NPT, NPTII kanamycin resistant gene

Vir: entire vir region of Ti plasmid of bacteria belonging to genus Agrobacterium

S Vir: entire vir region of Ti plasmid pTiBo542 of super virulent bacteria belonging to genus Agrobacterium

s vir*: fragment containing a part of vir region of Ti plasmid pTiBo542

BEST MODE FOR CARRYING OUT THE INVENTION

The method of the present invention for promoting efficiency of gene introduction into plant cells by a bacterium belonging to genus Agrobacterium, comprises centrifuging the plant cells or plant tissue. The plant cells or plant tissue may be contacted with the bacterium belonging to genus Agrobacterium under normal gravity after centrifuging the plant cells or tissue, or the plant cells or tissue may be contacted with the bacterium belonging to genus Agrobacterium while centrifuging the plant cells or tissue. Preferably, the plant cells or plant tissue are(is) contacted with the bacterium belonging to genus Agrobacterium under normal gravity after centrifuging the plant cells or tissue.

The conditions for centrifugation may appropriately be selected depending on the type of the plant used and the like, and may usually be carried out under a centrifugation acceleration of 100 G to 250,000 G, preferably 500 G to 200,000 G, more preferably 1000 G to 150,000 G. The time for centrifugation may appropriately be selected depending on the centrifugal acceleration, type of the plant used and so on, and is usually and preferably not less than one second. There is no upper limit of the centrifugation time, and about 10 minutes may usually be sufficient for attaining the object of the centrifugation. When the centrifugal acceleration is large, the efficiency of introducing genes may be significantly promoted even if the centrifugation time is very short, for example, 1 second or less. On the other hand, when the centrifugal acceleration is small, the efficiency of introducing genes may be significantly promoted by conducting the centrifugation for a long time. In most cases, especially preferred centrifugation conditions are about 500 G to 200,000 G, especially 1000 G to 150,000 G for about 1 second to 2 hours, and the appropriate centrifugation conditions for the particular plant cells or tissue may be easily selected by a routine experiment.

The method of the present invention is characterized by using the plant cells or plant tissue which were(was) centrifuged, or by contacting the plant cells or plant tissue with a bacterium belonging to the genus Agrobacterium while conducting centrifugation, and as the method for gene introduction or transformation per se using the bacterium belonging to the genus Agrobacterium, a well-known method may be applied as it is.

The method for gene introduction or transformation per se into plants using a bacterium belonging to the genus Agrobacterium is well-known in the art and is widely used.

It is known for a long time that a soil bacterium Agrobacterium (Agrobacterium tumefaciens) causes crown gall disease in a number of dicotyledons. In 1970s, it was discovered that Ti plasmid concerns the virulence, and that the T-DNA which is a part of Ti plasmid is incorporated into the plant genome. Thereafter, it was proved that the T-DNA contains genes participating in synthesis of hormones (cytokinins and auxins) required for induction of tumor, and that the genes are expressed in plants in spite of the fact that the genes are bacterial genes. A group of genes existing in the virulence region (vir region) in the Ti plasmid is required for the excision of T-DNA and its transfer to plants, and the border sequences existing at the both ends of the T-DNA are necessary for the T-DNA to be excised. Agrobacterium rhizogenes which is another bacterium belonging to the genus Agrobacterium has a similar system on the Ri plasmid (FIGS. 3 and 4).

Since T-DNA is incorporated into the plant genome by infection of Agrobacterium, it was expected that a desired gene may be incorporated into the plant genome by inserting the desired gene in the T-DNA. However, since Ti plasmid is as large as not less than 190 kb, it was difficult to insert a gene into the T-DNA by a standard technique of genetic engineering. Thus, a method for introducing a foreign gene into the T-DNA was developed.

First, disarmed strains such as LBA4404 (Hoekema et al., 1983 (Reference (12))), C58C1(pGV3850) (Zambryski et al., 1983 (Reference (40))), and GV3Ti11SE (Fraley et al., 1985 (Reference (9))), that have tumorigenic Ti plasmids from which hormone synthetase genes were eliminated, were prepared (FIG. 3). Two methods employing such a strain, that is, a method by which a desired gene is introduced into the Ti plasmid of Agrobacterium, and a method by which a T-DNA having a desired gene is introduced into Agrobacterium, were developed. One of these methods is the so called intermediate vector method (Fraley et al., 1985 (Reference (9)); Fraley et al., 1983 (Reference (10)); Zambryski et al., 1983 (Reference (40)), Japanese Laid-open Patent Application (Kokai) No. 59-140885 (EP116718)). In this method, an intermediate vector which is easy to handle by genetic manipulation techniques, in which a desired gene may be inserted, and which can be replicated in E. coli is introduced into the T-DNA in the disarmed type Ti plasmid of Agrobacterium by triparental mating (Ditta et al., 1980 (Reference (8))). Another method is the so called binary vector method (FIG. 3), which is based on the fact that although the vir region is necessary for the T-DNA to be incorporated into plants, it is not necessary that the T-DNA and the vir region exist in the same plasmid ((Hoekema et al., 1983). The vir region contains virA, virB, virC, virD, virE and virG (Plant Biotechnology Encyclopedia (Enterprise Co., Ltd. (1989)), and the vir region is defined as those containing all of virA, virB, virC, virD, virE and virG. Thus, the binary vector is a small plasmid which is replicable in both Agrobacterium and E. coli, and this plasmid is introduced into Agrobacterium having a disarmed type Ti plasmid. The introduction of the binary vector into Agrobacterium may be carried out by electroporation method, triparental mating or the like). Binary vector includes pBIN19 (Bevan, 1984(Reference (4))), pBI121(Jefferson, 1987(Reference (19))), pGA482(An et al., 1988(Reference (2)), Japanese Laid-open Patent Application (Kokai) No. 60-70080 (EP120516)), and a number of new binary vectors have been constructed based on these vectors. In the system of Ri plasmid, similar vectors have been constructed and are used for transformation.

Agrobacterium A281 (Watson et al., 1975 (Reference (39))) is a super-virulent strain, whose host spectrum is wide and whose efficiency of transformation is higher than other strains (Hood et al., 1987(Reference (13)); Komari, 1989 (Reference (21))). This feature is brought about by a Ti plasmid pTiBo542 contained in A281 (Hood et al., 1984 (Reference (16)); Jin et al., 1987 (Reference (20)); Komari et al., 1986 (Reference (24))).

Two new systems using pTiBo542 has been developed. One system utilizes strains EHA101 (Hood et al., 1986) and EHA105 (Hood et al., 1993) containing a Ti plasmid which is a disarmed type of pTiBo542. By applying these strains to the above-mentioned binary vector system, a system having a high efficiency of transformation was achieved, which is widely used for transformation of various plants. Another system is “super-binary” vector system (Hiei et al., 1994 (Reference (11)); Ishida et al., 1996 (Reference (18)); Komari et al., 1999 (Reference (26)), WO94/00977, WO95/06722) (FIG. 4). Since this system comprises a disarmed type Ti plasmid having the vir region (virA, virB, virC, virD, virE and virG) (each of these may also be hereinafter referred to as “vir fragment region”) and a plasmid having T-DNA, this is a kind of the binary vector system. However, it is different from the binary vector in that a super-binary vector (Komari, 1990a (Reference (22))) in which a vir region fragment (preferably a fragment containing at least virB or virG, more preferably a fragment at least containing virB and virG) substantially lacking at least one of the fragments of vir region is incorporated into the plasmid having the T-DNA, i.e., the binary vector. To introduce a T-DNA region into which a desired gene has been inserted into an Agrobacterium having the super-binary vector, homologous recombination via the triparental mating method may be employed as an easy method (Komari et al., 1996 (Reference (25))). It has been proved that the super-binary vector gives much higher transformation efficiency than the above-described various vector systems for a number of plant species (Hiei et al., 1994 (Reference (11)); Ishida et al., 1996 (Reference (18)); Komari, 1990b (Reference (23)); Li et al., 1996 (Reference (27)); Saito et al., 1992 (Reference (35))).

In the method of the present invention, the host bacterium belonging to the genus Agrobacterium is not restricted, and Agrobacterium tumefaciens (e.g., the above-described Agrobacterium tumefaciens LBA4404 (Hoekema et al., 1983 (Reference (12))) and EHA101 (Hood et al., 1986 (Reference (15))) may preferably be employed.

The method of the present invention may be applied to any of the gene introduction systems as long as it is based on the expression of the group of genes in the vir region in the bacterium belonging to the genus Agrobacterium so as to obtain significant effect. Thus, the method of the present invention may be applied to any of the vector systems such as the above-described intermediate vectors, binary vectors, super-virulent binary vectors and super-binary vectors so as to obtain the advantageous effect of the present invention. The method of the present invention may also be applied to the vector systems obtained by modification of these vectors (e.g., those wherein the entire or a part of the vir region of a bacterium belonging to the genus Agrobacterium is excised and additionally incorporated into the plasmid, or the entire or a part of the vir region of a bacterium belonging to the genus Agrobacterium is excised and is introduced into Agrobacterium as a part of a new plasmid). Further, needless to say, by the method of the present invention, the efficiency of introduction of the T-DNA region of wild type Agrobacterium is promoted so as to promote the infection efficiency.

The desired gene to be introduced into the plant may be inserted into a restriction site in the T-DNA region of the above-described plasmid by a conventional method, and the Agrobacterium into which the desired gene was incorporated may be selected based on an appropriate selection marker such as a drug resistant gene against a drug such as kanamycin or paromomycin. In cases where the plasmid is large and has a number of restriction sites, it is not always easy to insert the desired DNA into the T-DNA region by an ordinary subcloning method. In such a case, the desired DNA may be inserted by the triparental mating method utilizing the homologous recombination in the cell of the bacterium belonging to the genus Agrobacterium.

Introduction of the plasmid into a bacterium belonging to the genus Agrobacterium such as Agrobacterium tumefaciens may be carried out by a known method including the above-mentioned triparental mating method, electroporation method, electroinjection method and chemical treatments with PEG or the like.

The gene which is to be introduced into the plant is, in principle, arranged between the left and right border sequences of the T-DNA as in the conventional method. However, since the plasmid is annular, the plasmid may contain only one border sequence. Alternatively, in cases where a plurality of genes are to be arranged at different sites, the plasmid may contain three or more border sequences. Alternatively, arrangement of the desired plasmid in the Ti or Ri plasmid may be performed in the cell of the bacterium belonging to the genus Agrobacterium, or the desired gene may be arranged in another plasmid. Further, the desired gene may be arranged in a plurality of types of plasmids.

Introduction of a gene into the plant cells via a bacterium belonging to the genus Agrobacterium may be attained by simply making the plant cells or plant tissue contact the bacterium belonging to the genus Agrobacterium. For example, a cell suspension of the bacterium belonging to the genus Agrobacterium having a population density of about 10⁶ to 10¹¹ cells/ml is prepared, and the plant cells or the plant tissue are(is) immersed in the suspension for about 3 to 10 minutes, followed by co-culturing the resultant on a solid medium for several days, thereby attaining the introduction of the gene.

The cells or the tissue to be subjected to the gene introduction are(is) not restricted at all and may be a leaf, root, stem, fruit or any other portion of the plant. Further, dedifferentiated tissue such as a callus or a non-dedifferentiated tissue such as an embryo may be employed. The type of the plant is not restricted at all, and angiosperms are preferred. As long as the plant is an angiosperm, either dicotyledon or monocotyledon is preferred.

As will be concretely shown in the following Examples, by the method of the present invention, the efficiency of gene introduction is significantly promoted when compared with the conventional Agrobacterium method.

EXAMPLES

The present invention will now be described by way of examples thereof. It should be noted that the present invention is not restricted to the following Examples.

Example 1 (1) Agrobacterium Strains and Plasmids

As the Agrobacterium and its vectors, LBA4404(pBI121) (pBI121 is commercially available from CLONETECH, U.S., (Jefferson R A 1987 (Reference (19))), LBA4404 (pIG121Hm) (Hiei, Y. et al., 1994 (Reference (11)), LBA4404 (pTOK233) (Hiei et al., 1994 (Reference (11))) and LBA4404 (pSB133) (FIG. 2) were used.

Construction of pSB133 was carried out as follows: A DNA fragment having a size of 6.2 kb obtained by digesting pGA482 (An G et al., 1985 (Reference (3))) with a restriction enzyme SalI was ligated to a DNA fragment with a size of 5.1 kbp obtained by digesting pSB11 (Komari et al., 1996 (Reference (25)) with SalI to prepare a plasmid. This plasmid was then digested with restriction enzymes Eco RI and BglII to obtain a DNA fragment with a size of 8.6 kb. This DNA fragment was blunted and a BglII linker (commercially available from TaKaRa) was inserted therein to obtain a plasmid pSB27. The pSB27 was digested with a restriction enzyme HindIII, and a DNA fragment with a size of 3.1 kb containing 35S promoter and an intron-GUS gene, which fragment was obtained by digesting pIG221 (Ohta S et al., 1990 (Reference (32)), was inserted therein to obtain pSB33. The pSB33 was introduced into E. coli LE392, and then introduced into Agrobacterium LBA4404 containing pSB1 (Komari et al., 1996 (Reference (25))) by triparental mating method (Ditta G et al., 1980 (Reference (8)). The pSB133 was obtained by homologous recombination between pSB1 and pSB33 in the cell of Agrobacterium. The T-DNA region of pBI121 contains a kanamycin-resistant gene (nptII) controlled by the promoter of nopaline synthetase gene (nos) and a GUS gene controlled by 35S promoter of cauliflower mosaic virus (CaMV). Each of the T-DNA regions of pIG121Hm and pTOK233 contains an nptII gene controlled by nos promoter, an hpt gene controlled by 35S promoter, and a GUS gene controlled by the 35S promoter, which GUS gene contains introns of the catalase gene of castor bean. The T-DNA region of pSB133 contains an nptII gene controlled by nos promoter and a GUS gene controlled by 35S promoter of CaMV, which GUS gene contains introns of the catalase gene of castor bean (FIG. 2). The plasmids pSB133 and pTOK233 are super-binary vectors having high abilities of transformation (Komari, T. et al., 1999 (Reference (26))).

(2) Sample Varieties and Tissues

As the sample varieties, Koshihikari and Tsukinohikari, which are Japonica rice varieties, were used. Glumes of immature seeds at 8 to 14 days after flowering were removed and the seeds were sterilized with 70% ethanol for several seconds and with 1% aqueous sodium hypochlorite solution containing Tween 20 for 15 minutes. After washing the seeds several times with sterilized water, immature embryos with lengths of 1.5 to 2 mm were excised and used as the sample tissue.

(3) Centrifugation Treatment

The immature embryos of rice were placed in tubes containing sterilized water and centrifuged under an acceleration of 760 G to 150,000 G using a micro high-speed centrifuge, large high-speed centrifuge or an ultra high-speed centrifuge. After the centrifugation, the immature embryos were infected with Agrobacterium.

(4) Infection and Co-Culturing

The method for infection to the immature embryos and the method for co-culturing were in accordance with the methods by Hiei et al. (1994) (Reference (11)). That is, after the centrifugation, the sterilized water in each tube was removed and suspension of Agrobacterium was added, followed by stirring the mixture with a vortex mixer for 5 to 30 seconds.

The suspensions of bacteria were prepared by collecting colonies of Agrobacterium cultured on AB medium (Chilton, M-D et al., 1974 (Reference (6))) with a platinum loop and suspending the collected bacteria in modified AA medium (AA major inorganic salts, AA amino acids and AA vitamins (Toriyama K. et al., 1985 (Reference (36)), MS minor salts (Murashige, T et al., 1962 (Reference (30)), 1.0 g/l casamino acid, 100 μM acetosyringone, 0.2 M sucrose, 0.2 M glucose). After leaving the mixture of immature embryos and the suspension of Agrobacterium to stand at room temperature for about 5 minutes, the immature embryos were plated on a medium for co-culturing. As the medium for co-culturing, 2N6-AS medium (Hiei et al. 1994 (Reference (11))) was used except that the inorganic salts thereof were changed to the composition of R2 medium (Ohira et al. 1973 (Reference (31)). It should be noted, however, that the major inorganic salts (KNO₃, KH₂PO₄, CaCl₂2H₂O, MgSO₄7H₂O) were added to the medium to half concentrations. The density of the bacterial cells to be infected was adjusted to 1×10⁸ to 1×10⁹ cfu/ml. The co-culturing was carried out for 3 to 13 days, and a portion of the immature embryo was treated with X-Gluc to check the expression of the GUS gene (Hiei et al. 1994) (Reference (11)). That is, immediately after the co-culturing, the tissue was immersed in 0.1M phosphate buffer (pH 6.8) containing 0.1% Triton X-100, and was left to stand at 37° C. for 1 hour. After removing Agrobacterium with phosphate buffer, phosphate buffer containing 1.0 mM 5-bromo-4-chloro-3-indolyl-β-D-glucuronic acid (X-gluc) and 20% methanol was added. After incubating the resultant at 37° C. for 24 hours, tissueds colored in blue were observed under microscope.

(5) Selection of Transformed Cells

After the co-culturing, the immature embryos and calli were transferred to a primary selection medium containing 250 mg/l carbenicillin and 250 mg/l cefotaxime, and further containing 200 mg/l paromomycin or 10 to 30 mg/l hygromycin, and cultured at 30° C. under luminous condition for 1 to 2 weeks. As the primary selection medium, 2N6K medium described in Hiei et al. (1994) (Reference (11)) supplemented with D-sorbitol to 30 g/l was used (K medium). Further, a medium (N medium) which was the same as the 2N6 medium (inorganic salts and vitamins of N6 (Chu C. C. 1978 (Reference (7))), 1 g/l casamino acid, 2 mg/l 2,4-D) except that the concentration of (NH₄)₂SO₄ was changed to 232 mg/l and that the amino acids of AA medium (Toriyama et al., 1985 (Reference (36)) were supplemented was also used in the test.

The calli formed on the primary selection medium were transferred to a secondary selection medium containing 250 mg/l cefotaxime and 250 mg/l carbenicillin, and further containing 200 mg/l paromomycin or 80 mg/l hygromycin, and cultured at 30° C. under luminous condition for 1 to 2 weeks. As the secondary selection medium, a medium which was the same as N6-7 medium described in Hiei et al. (1994) (Reference (11)) except that the concentration of (NH₄)₂SO₄ was changed to 232 mg/l and that the amino acids of AA medium (Toriyama et al., 1985 (Reference (36)) were supplemented was used. To the primary and secondary selection media containing paromomycin, agarose was added to 8 g/l as a solidifier. The rate of emerged resistant calli was investigated after the secondary selection.

(6) Regeneration of Transformants

The calli resistant to the selection drugs, obtained from the scutella of immature embryos were plated on N6S3 medium (Hiei et al. 1994 (Reference (11)) for regeneration containing 250 mg/l carbenicillin and 250 mg/l cefotaxime, and further containing 100 mg/l paromomycin or 50 mg/l hygromycin.

(7) Checking GUS Expression in Regenerated Plants

Leaves of the regenerated plants resistant to the drugs, obtained by culturing for regeneration at 25° C. under luminous condition for 4 to 5 weeks were checked for the expression of GUS gene by treating them with X-Gluc in the same manner as mentioned above (Hiei et al. 1994 (Reference (11)). The regenerated plants were transplanted to 500-fold diluted aqueous Hyponex solution and cultivated at 25° C. under luminous condition for about 2 weeks, followed by transplantation to pots in a green house.

(8) Results

(i) Discussion about Effects by Centrifugation Treatment

Using a micro high-speed centrifuge, large high-speed centrifuge and an ultra high-speed centrifuge, the effect by the centrifugation treatment to the rice immature embryos was tested. As a result, the efficiency of gene introduction was promoted when the acceleration was within the range of 10 KG to 100 KG (Tables 1, 2, 3 and 6). As for the treatment time, advantageous effect was clearly observed with the treatment for 10 minutes (Tables 4 and 5). The frequency of the transient expression of GUS was not different between the varieties, that is, between Koshihikari and Tsukinohikari. Since not only the effect for promoting the efficiency of gene introduction, but also the effect for inducing formation of callus was observed, it was suggested that centrifugation treatment is effective for induction and growth of calli and in the culturing of plants including other species.

As shown in Table 6, induction of calli from the immature embryos of

Tsukinohikari was not at all observed when the centrifugation was carried out at 250 KG for 60 minutes using the ultra high-speed centrifuge. However, induction of calli was observed when the centrifugation was carried out at 110 KG for 60 minutes, and expression of GUS was also observed at high rate. Similarly, as for Koshihikari, induction of calli from the immature embryos of Tsukinohikari was not at all observed when the centrifugation was carried out at 250 KG for 60 minutes using the ultra high-speed centrifuge. From these results, the advantageous effect by centrifugation for rice immature embryo is thought to be obtained at an acceleration between 5 KG to 200 KG. Thus, in view of the simplicity of the treatment, when a micro high-speed centrifuge or a large high-speed centrifuge is used, the treatment at 20 KG or 40 KG is thought to be appropriate. Further, as shown in Tables 9, 10 and 11, it was proved that by the centrifugation treatment at 20 KG for 60 minutes, transformation using immature embryo may be attained not only for LBA4404 (pSB133) having a super-binary vector known to have a high transformation ability, but also for LBA4404 (pIG121Hm) containing an ordinary binary vector.

(ii) Discussion about Centrifugation Treatment and Duration of Co-Culturing

As shown in Tables 7 and 8, the efficiency of GUS expression observed in the transient assay was higher when the duration of co-culturing was 6 or 13 days than when the duration of co-culturing was 3 days. In another experiment, a high GUS expression was observed when the duration of co-culturing was 9 days. Various immature embryos which underwent different durations of co-culturing are now cultured on a primary selection medium (10 ppm hygromycin, 200 ppm paromomycin), and there is a tendency that the rate of emerging of drug resistant calli is smaller in the group co-cultured for 9 or 13 days than in the group co-cultured for 3 or 6 days.

(iii) Examination of Efficiency of Transformation by Centrifugation Treatment

At present, the GUS-positive transformants (Tables 4 and 5) prepared as described above are acclimatized, and culturing is continued. For some lines, seeds were collected and fertility was checked. As a result, no differences in morphology and fertility between the centrifuged transformants and the non-treated transformants (Koshihikari and Tsukinohikari) were observed.

Hiei et al. (1994 (Reference (11))) reported that transformation may be attained with a relatively high efficiency using calli of rice. Aldemita R R et al. 1996 (Reference (1))) reported a case of transformation using rice immature embryo. To more effectively and more stably carry out these transformation methods, the above-described centrifugation treatment method is very effective. Especially, although the quality of immature embryo is likely varied depending on the environment of culturing so that it is not easy to always obtain immature embryo suited for transformation, it may be possible to keep high efficiency of transformation by subjecting the immature embryo to the centrifugation treatment. Hiei et al. (1994) (Reference (11)) showed that a super-binary vector having a high transformation ability promotes the efficiency of transformation of rice. According to Aldemita R R et al. 1996 (Reference (1))), transformants were obtained only in the test using LBA4404 (pTOK233) containing a super-binary vector. By the centrifugation treatment method according to the present invention, even when an ordinary binary vector is used, a high efficiency of transformation is attained, which is comparable to or even higher than that attained in the transformation using a super-binary vector. Further, by employing both the super-binary vector and the centrifugation treatment method, the efficiency may be even more promoted. Still further, it is expected that transformants may be obtained by employing the centrifugation treatment method for the varieties with which a transformant has not hitherto been obtained.

TABLE 1 Various Centrifugation Treatments and Results of GUS Expression after Co-culturing (Sample Strain: LBA4404/pSB133) Population Density of Infected Bacterium Not Centrifugal Acceleration Variety (cfu/ml) Treated 760 G 8,500 G 19,100 G Koshihikari 1 × 10⁸ 3/10(+) 6/10(+) 7/10(++) 7/10(+++) 1 × 10⁹ 2/10(+)  0/10(—) 4/10(++) 7/10(+++) Tsukino- 1 × 10⁸ 4/10(+) 3/10(+)  9/10(+++) 7/10(+++) hikari 1 × 10⁹ 1/10(+)  6/10(++) 2/10(+)  7/10(+++) Time of Centrifugation Treatment: 10 minutes; Duration of Co-culturing: 3 to 5 days; Number of GUS-positive immature embryos/Number of sample immature embryos The symbols in parentheses indicate the area of the region in scutella in which GUS was expressed. —: none; +: small; ++: medium; +++: large

TABLE 2 Rate of Emerging of Paromomycin-resistant Calli from Koshihikari Immature Embryos (Sample Strain: LBA4404/pSB133) Population Density of Infected Selection Bacterium Not Centrifugal Acceleration Medium (cfu/ml) Treated 760 G 8,500 G 19,100 G N 1 × 10⁸ 4.8%(1/21) 0.0%(0/22) 15.0%(3/20) 31.8%(7/22) medium 1 × 10⁹ 4.3%(1/23) 4.5%(1/22) 16.7%(3/18) 13.3%(2/15) K 1 × 10⁸ 0.0%(0/21) 0.0%(0/22) 14.3%(3/21) 18.2%(4/22) medium 1 × 10⁹ 0.0%(0/23) 0.0%(0/21)  0.0%(0/19)  0.0%(0/22) Number of immature embryos from which resistant calli were derived/Number of sample immature embryos, checked after completion of the secondary selection Time of Centrifugation Treatment: 10 minutes; Duration of Co-culturing: 3 to 5 days

TABLE 3 Rate of Emerging of Paromomycin-resistant Calli from Tsukinohikari Immature Embryos (Sample Strain: LBA4404/pSB133) Population Density of Infected Selection Bacterium Not Centrifugal Acceleration Medium (cfu/ml) Treated 760 G 8,500 G 19,100 G N 1 × 10⁸ 0.0%(0/11) 0.0%(0/11) 30.0%(3/10) 36.4%(4/11) medium 1 × 10⁹ 0.0%(0/11) 9.1%(1/11) 27.3%(3/11) 54.5%(6/11) K 1 × 10⁸ 0.0%(0/10) 0.0%(0/15)  9.1%(1/11)  9.1%(1/11) medium 1 × 10⁹ 0.0%(0/11) 0.0%(0/11)  0.0%(0/11) 45.5%(5/11) Number of immature embryos from which resistant calli were derived/Number of sample immature embryos, checked after completion of the secondary selection Time of Centrifugation Treatment: 10 minutes; Duration of Co-culturing: 3 to 5 days

TABLE 4 Time of Centrifugation Treatment and Results of GUS Expression after Co-culturing Time of Centrifugation Treatment Strains and Not 10 30 60 Plasmids Treated minutes minutes minutes LBA4404(pSB133) 9/10(+)  9/10(++) 10/10(++) 10/10(+++) LBA4404(pTOK233) 9/10(+) 10/10(++) 10/10(++) 10/10(+++) Centrifugal acceleration: 20,000 G; Sample Variety: Koshihikari; Number of GUS-positive immature embryos/Number of sample immature embryos area of the region in scutella in which GUS was expressed. +: small; ++: medium; +++: large

TABLE 5 Time of Centrifugation Treatment and Rate of Emerging of Paromomycin-resistant Calli (Variety: Koshihikari) Time of Centrifugation Treatment Selection Culturing Not 10 30 60 Medium Condition Treated minutes minutes minutes N Luminous 0.0%(0/31) 34.3%(12/35) 35.0%(14/40) 53.3%(16/30) medium (30° C.) Dark 0.0%(0/32) 54.1%(20/37) 34.2%(13/38) 58.6%(17/29) (30° C.) K Luminous 0.0%(0/31) 20.0%(7/35)  38.5%(15/39) 40.0%(12/30) medium (30° C.) Dark 0.0%(0/32) 48.6%(17/35) 41.0%(16/39) 33.3%(10/30) (30° C.) Centrifugal acceleration: 20,000 G; Duration of Co-culturing: 3 to 5 days, checked after completion of the secondary selection Number of immature embryos from which resistant calli were derived/Number of sample immature embryos

TABLE 6 Intensity of Centrifugation Treatment and GUS Expression after Co-culturing (variety: Tsukinohikari) Duration Number of Immature Embryos Centrifugation of Co- Frequency of GUS Expression in Scutella Treatments culturing — ± + ++ Not Treated 3 days 6 4 0 0 6 days 0 2 6 2  20 KG ¹⁾ 3 days 0 0 2 8 6 days 0 0 2 8  40 KG ²⁾ 3 days 1 0 1 8 6 days 0 0 0 10 110 KG ³⁾ 3 days 1 0 5 4 6 days 0 0 2 8 250 KG ³⁾ 3 days 10 0 0 0 6 days 10 0 0 0 Sample Strain: LBA4404/pIG121Hm; Time of Centrifugation Treatment: 60 minutes ¹⁾ micro high-speed centrifuge; ²⁾ large high-speed centrifuge; ³⁾ ultra high-speed centrifuge Rate of GUS-expressed area in scutella: —: none; ±: <⅛; +: ⅛-¼; ++: >¼

TABLE 7 Centrifugation Treatment, Duration of Co-culturing and GUS Expression after Co-culturing (Variety: Tsukinohikari) Duration Number of Immature Embryos Centrifugation of Co- Frequency of GUS Expression in Scutella Treatments culturing — ± + ++ Not Treated 3 days 5 4 1 0 6 days 0 6 2 2 13 days  0 5 2 3 20 KG ¹⁾ 3 days 0 2 5 3 6 days 0 1 3 6 13 days  0 1 3 6 40 KG ²⁾ 3 days 0 1 7 2 6 days 0 0 8 2 13 days  0 1 5 4 Sample Strain: LBA4404/pIG121Hm; ¹⁾ micro high-speed centrifuge; ²⁾ large high-speed centrifuge; Centrifugation was carried out for 60 minutes at the indicated revolution. Rate of GUS-expressed area in scutella: —: none; ±: <⅛; +: ⅛-¼; ++: >¼

TABLE 8 Centrifugation Treatment, Duration of Co-culturing and GUS Expression after Co-culturing (Variety: Koshihikari) Duration Number of Immature Embryos Centrifugation of Co- Frequency of GUS Expression in Scutella Treatments culturing — ± + ++ Not Treated 3 days 7 3 0 0 6 days 3 1 0 0 13 days  1 6 2 1 20 KG ¹⁾ 3 days 0 0 1 9 6 days 0 0 2 8 13 days  0 0 1 9 40 KG ²⁾ 3 days 1 0 4 5 6 days 0 0 0 10 13 days  0 0 1 9 Sample Strain: LBA4404/pIG121Hm; ¹⁾ micro high-speed centrifuge; ²⁾ large high-speed centrifuge; Centrifugation was carried out for 60 minutes at the indicated revolution. Rate of GUS-expressed area in scutella: —: none; ±: <⅛; +: ⅛-¼; ++: >¼

TABLE 9 Results of Transformation by LBA4404(pBI121) (Variety: Tsukinohikari) Number of Number of Number of Transfor- Immature Acclimatized GUS-positive mation Treatments Embryos Plants Plants Efficiency Not Treated 50 17 12 24.0(%) Centrifugation 150 60 54 36.0(%) Treatment Centrifugation Treatment: 20 KG-60 minutes; Duration of Co-culturing: 5 days

TABLE 10 Results of Transformation by LBA4404(pIG121Hm) (Variety: Tsukinohikari) Number of Number of Number of Transfor- Immature Acclimatized GUS-positive mation Treatments Embryos Plants Plants Efficiency Not Treated 40 9 3  7.5(%) Centrifugation 47 10 5 10.6(%) Treatment Centrifugation Treatment: 20 KG-60 minutes; Duration of Co-culturing: 5 days

TABLE 11 Results of Transformation by LBA4404(pBI121) (Variety: Koshihikari) Number of Number of Number of Transfor- Immature Acclimatized GUS-positive mation Treatments Embryos Plants Plants Efficiency Not Treated 49 4 2 4.1(%) Centrifugation 274 35 27 9.9(%) Treatment Centrifugation Treatment: 20 KG-60 minutes; Duration of Co-culturing: 5 days

TABLE 12 Results of Transformation by LBA4404(pSB133) (Variety: Koshihikari) Number of Number of Number of Transfor- Immature Acclimatized GUS-positive mation Treatments Embryos Plants Plants Efficiency Not Treated 63 0 — 0.0(%) Centrifugation 281 30 23 8.2(%) Treatment Centrifugation Treatment: 20 KG-60 minutes; Duration of Co-culturing: 3 days

Example 2

Immature embryos of maize with a size of about 1.2 mm (variety: A188, obtained from National Institute of Agrobiological Resources, The Ministry of Agriculture, Forestry and Fisheries) were aseptically collected and washed once with LS-inf liquid medium. To a centrifugal tube containing the immature embryo and 2.0 ml of LS-inf medium containing 100 μM acetosyringone, a suspension of Agrobacterium tumefaciens LBA4404(pSB131) (Ishida et al. 1996 (Reference (18))) was added to a population density of about 1×10⁹ cfu/ml, and the resulting mixture was centrifuged at 40,000 G, at 4° C. for 30 minutes. The control embryo was left to stand in the same cell suspension at room temperature for 30 minutes. After the treatment, the mixture was gently stirred and plated on LS-AS medium such that the surface of hypocotyl contacts the medium. On the other hand, infection to immature embryos after centrifugation treatment was carried out as follows: Embryos aseptically collected were washed once with LS-inf liquid medium and transferred to centrifugation tubes containing the same medium., followed by centrifugation treatment at 20 KG or 40 KG at 4° C. for 1 hour. The control sample was left to stand in the liquid medium at room temperature for 1 hour. After the treatment, the liquid medium was removed, and a suspension of LBA4404 (pSB131) with a population density of about 1×10⁹ cfu/ml was added, followed by gently stirring of the mixture. After leaving the mixture to stand at room temperature for 5 minutes, the embryos were plated on LS-AS medium containing 10 μM AgNO₃ such that the surface of each hypocotyl contacts the medium. After co-culturing in the dark at 25° C. for 3 days, an aliquot of the immature embryos was sampled and the transient expression of the GUS gene was checked by the treatment with X-gluc as in Example 1. The above-described medium and method for culturing were in accordance with Ishida, Y. et al. 1996 (Reference (18)).

The transient expression of the GUS gene in the A188 immature embryos infected with LBA4404 (pSB131) is shown in Table 13. Although any embryo showed expression of the GUS gene, a number of the immature embryos subjected to the centrifugation treatment showed expression in larger area than the control immature embryos. The increase in the gene-introduced sites by the centrifugation treatment was observed in both cases wherein the centrifugation treatment was performed together with the Agrobacterium and wherein the Agrobacterium was infected after the centrifugation treatment. Further, expression of the GUS gene was observed in larger area than in the control even if the intensity of centrifugation and the time of treatment were changed.

By these results, the possibility that by culturing the immature embryos after centrifugation treatment on a selection medium, transformed plants are obtained at higher efficiency than the control was suggested. Further, the possibility that the maize varieties (Ishida et al. 1996 (Reference (18))) other than A188, which could not be hitherto transformed by the conventional Agrobacterium method, may be transformed by the centrifugation treatment, was suggested.

TABLE 13 Transient Expression of GUS Gene in A188 Immature Embryos Number of Sample Treatment Immature Expression of GUS Gene Test KG min Embryos +++ ++ + − 1 40 30 27 7 10 10 0 Control 30 30 1 17 12 0 2 40 60 20 0 3 17 0 20 60 20 0 10 10 0 Control 60 20 0 1 19 0 Control was treated under 1G In Test 1, centrifugation treatment was performed in the presence of Agrobacterium. In Test 2, Agrobacterium was infected after the centrifugation treatment.

REFERENCES

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1. A method for transforming a monocotyledonous plant or plant tissue with a desired gene comprising: centrifuging the monocotyledonous plant tissue or the plant; under a centrifugal acceleration of 1000 G to 150,000 G; and contacting the monocotyledonous plant or plant tissue with Agrobacterium, wherein said Agrobacterium includes the desired gene, and wherein said centrifugation promotes efficiency of the transformation of the desired gene into said tissue or plant, said contacting step is carried out after or simultaneously to said centrifugation.
 2. The method according to claim 1, wherein said plant tissue or said plant belongs to the family Gramineae.
 3. The method according to claim 2, wherein said plant tissue or said plant is rice or maize.
 4. The method according to claim 1, wherein said contacting is carried out after centrifuging said plant tissue or said plant.
 5. The method according to claim 4, wherein said centrifugation is carried out for 1 second to 4 hours.
 6. The method according to claim 5, wherein said centrifugation is carried out for 5 minutes to 2 hours.
 7. A method for transforming a plant or plant tissue with a desired gene comprising: centrifuging from 5 minutes to 2 hours a plant or plant tissue from rice or maize under a centrifugal acceleration of 1000 G to 150,000 G; and contacting said plant or plant tissue with Agrobacterium, wherein said Agrobacterium includes the desired gene, and wherein said centrifugation promotes efficiency of the transformation of the desired gene into said tissue or plant, said contacting step is carried out after or simultaneously to said centrifugation.
 8. Plant cells, a plant tissue or a plant prepared by the method according to claim
 1. 9. Cells of a plant belonging to family Gramineae, tissue of a plant belonging to family Gramineae, or a plant belonging to family Gramineae prepared by the method according to claim
 2. 10. Rice cells, rice tissue, rice, maize cells, maize tissue or maize prepared by the method according to claim
 3. 